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MB Sample ID: SA154483

Local Sample ID:CTRL_2
Subject ID:SU001751
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606

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Combined analysis:

Analysis ID AN002732
Analysis type MS
Chromatography type HILIC
Chromatography system Shimadzu Prominence UFPLC xr system
Column HILIC Kinetex (50 x 2.1mm,2.6um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Orbitrap Elite Hybrid Ion Trap-Orbitrap
Ion Mode POSITIVE
Units intensities

Chromatography:

Chromatography ID:CH002018
Chromatography Summary:Lipid extracts (2 μL injection volume in ChCl3:MeOH 2:1) were separated over an 8 minutes gradient at a flow rate of 200 μL/min on a HILIC Kinetex Column (2.6lm, 2.1 × 50 mm2) on a Shimadzu Prominence UFPLC xr system (Tokyo, Japan). Mobile phase A was acetonitrile:methanol 10:1 (v/v) containing 10 mM ammonium formate and 0.5% formic acid while mobile phase B was deionized water containing 10 mM ammonium formate and 0.5% formic acid. The elution of the gradient began with 5% B at a 200 μL/min flow and increased linearly to 50% B over 7 min, then the elution continued at 50% B for 1.5 min and finally, the column was re-equilibrated for 2.5 min.
Instrument Name:Shimadzu Prominence UFPLC xr system
Column Name:HILIC Kinetex (50 x 2.1mm,2.6um)
Flow Gradient:The elution of the gradient began with 5% B and increased linearly to 50% B over 7 min, then the elution continued at 50% B for 1.5 min and finally, the column was re-equilibrated for 2.5 min.
Flow Rate:200 µL/min
Solvent A:91% acetonitrile/9% methanol; 0.5% formic acid; 10 mM ammonium formate
Solvent B:1005 water; 0.5% formic acid; 10 mM ammonium formate
Chromatography Type:HILIC
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